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The Antihypertensives and Vascular, Endothelial and Cognitive Function Trial (AVEC)
This study is currently recruiting participants.
Verified by National Institute on Aging (NIA), September 2009
First Received: January 11, 2008   Last Updated: September 9, 2009   History of Changes
Sponsor: National Institute on Aging (NIA)
Collaborator: Hebrew SeniorLife
Information provided by: National Institute on Aging (NIA)
ClinicalTrials.gov Identifier: NCT00605072
  Purpose

The purpose of this study is to examine the effects of blood pressure medications on cognition and blood flow in hypertensive elderly patients with cognitive impairment. The hypothesis is that treatment with an angiotensin receptor blocker (ARB) or an angiotensin-converting enzyme inhibitor (ACEI) will be associated with a slower rate of further cognitive decline, improved cerebral blood flow and its regulation, and preserved physical function as compared to treatment with a diuretic (HCTZ), independent of blood pressure level.


Condition Intervention Phase
Cognitive Impairment
Hypertension
Aging
Drug: candesartan
Drug: lisinopril
Drug: hydrochlorothiazide
Drug: nifedipine, long acting
Drug: metoprolol, long-acting
Phase II

Study Type: Interventional
Study Design: Treatment, Randomized, Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Parallel Assignment, Efficacy Study
Official Title: The Antihypertensives and Vascular, Endothelial and Cognitive Function Trial (AVEC Trial)

Resource links provided by NLM:


Further study details as provided by National Institute on Aging (NIA):

Primary Outcome Measures:
  • Cognitive assessment measured by Trail Making Test, Hopkins Verbal Learning Test - Revised (HVLT-R), and Digit Span Test [ Time Frame: Baseline, 1, 6, and 12 months ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Changes in Cerebral Blood Flow (CBF) and cerebral vasoreactivity [ Time Frame: Baseline, then 6 and 12 months after BP control ] [ Designated as safety issue: No ]
  • Endothelial function assessed using the flow mediated dilatation (FMD) procedure [ Time Frame: Baseline, then 6 and 12 months after BP control ] [ Designated as safety issue: No ]
  • Biochemical measurement to monitor for adverse events: hyperkalemia, renal failure, leukopenia and liver function abnormalities [ Time Frame: Baseline, 2-4 weeks, 2, 4, 9, and 12 months ] [ Designated as safety issue: Yes ]

Estimated Enrollment: 100
Study Start Date: January 2008
Estimated Study Completion Date: December 2011
Estimated Primary Completion Date: December 2011 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
ARB: Experimental
Angiotensin Receptor Blocker
Drug: candesartan
orally 8 mg increased to 16 mg then 32 mg to achieve target blood pressure of 140/90, then daily for 12 months
Drug: nifedipine, long acting
If needed to achieve target blood pressure of 140/90, added to ARB or ACEI at 30 mg increased to 60 mg and 90 mg in 2 week increments
Drug: metoprolol, long-acting
If needed to achieve target blood pressure of 140/90, added to ARB or ACEI at 12.5 mg increased to 25 mg and 50 mg
ACEI: Experimental
Angiotensin-Converting Enzyme (ACE) Inhibitor
Drug: lisinopril
orally 10 mg increased to 20 mg then 40 mg to achieve target blood pressure of 140/90, then daily for 12 months
Drug: nifedipine, long acting
If needed to achieve target blood pressure of 140/90, added to ARB or ACEI at 30 mg increased to 60 mg and 90 mg in 2 week increments
Drug: metoprolol, long-acting
If needed to achieve target blood pressure of 140/90, added to ARB or ACEI at 12.5 mg increased to 25 mg and 50 mg
HCTZ: Active Comparator Drug: hydrochlorothiazide
orally 12.5 mg increased to 25 mg to achieve target blood pressure of 140/90, then daily for 12 months

Detailed Description:

There is mounting evidence that hypertension, which affects more than 65% of the US elderly population, accelerates cognitive decline and increases the risk of functional disability among older individuals. Hypertension is also associated with cerebral blood flow reduction and dysregulation which contribute to further cognitive and functional impairment. Drugs that inhibit angiotensin II (ACEI and ARB) are commonly used antihypertensives and may have a protective effect on cognitive function, cerebral blood flow and physical function compared to other antihypertensives such as hydrochlorothiazide (HCTZ).

A total of 100 individuals will be recruited for this pilot 3-arm randomized study to investigate the effects of: (i) 12 months treatment with candesartan (ARB) compared to hydrochlorothiazide (HCTZ) and (ii) 12 months treatment with lisinopril (ACEI) compared to HCTZ and (iii) to estimate the effect size difference between lisinopril and losartan on cognition, cerebral blood flow regulation, and functional measures in a sample of elderly hypertensive individuals with objective evidence of cognitive impairment.

  Eligibility

Ages Eligible for Study:   60 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • 60 years or older
  • Hypertension
  • Cognitive criteria: score either 10 or less out of 15 for the executive clock draw test 1 (CLOX1) or less than or equal to 1 standard deviation from the corresponding age specific mean on the immediate memory subtest

Exclusion Criteria:

  • Intolerance to ACEI or ARB
  • History of congestive heart failure
  • History of diabetes mellitus
  • History of stroke (less than 6 months)
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00605072

Contacts
Contact: Meaghan Hart 617-363-8484 MeaghanHart@hrca.harvard.edu

Locations
United States, Massachusetts
Institute for Aging Research at Hebrew SeniorLife Recruiting
Boston, Massachusetts, United States, 02131
Contact: Meaghan Hart     617-363-8484     MeaghanHart@hrca.harvard.edu    
Principal Investigator: Ihab Hajjar, MD, MS            
Sub-Investigator: Lewis Lipsitz, MD            
Sponsors and Collaborators
Hebrew SeniorLife
Investigators
Principal Investigator: Ihab Hajjar, MD Hebrew SeniorLife
  More Information

Publications:
Responsible Party: Hebrew SeniorLife ( Ihab Hajjar, MD )
Study ID Numbers: IA0127, 1K23AG30057-01A1
Study First Received: January 11, 2008
Last Updated: September 9, 2009
ClinicalTrials.gov Identifier: NCT00605072     History of Changes
Health Authority: United States: Federal Government

Keywords provided by National Institute on Aging (NIA):
cognitive disorders

Additional relevant MeSH terms:
Vasodilator Agents
Neurotransmitter Agents
Adrenergic Agents
Molecular Mechanisms of Pharmacological Action
Cardiotonic Agents
Sodium Chloride Symporter Inhibitors
Diuretics
Physiological Effects of Drugs
Calcium Channel Blockers
Reproductive Control Agents
Nifedipine
Membrane Transport Modulators
Tocolytic Agents
Mental Disorders
Therapeutic Uses
Angiotensin-Converting Enzyme Inhibitors
Adrenergic beta-Antagonists
Cardiovascular Diseases
Anti-Arrhythmia Agents
Sympatholytics
Lisinopril
Vascular Diseases
Enzyme Inhibitors
Cardiovascular Agents
Metoprolol
Antihypertensive Agents
Protective Agents
Hydrochlorothiazide
Cognition Disorders
Pharmacologic Actions

ClinicalTrials.gov processed this record on November 27, 2009